No abstract available
Publication types
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Case Reports
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English Abstract
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Letter
MeSH terms
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Child Behavior Disorders / etiology
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Comorbidity
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Diagnosis, Differential
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Epilepsies, Myoclonic / complications*
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Epilepsies, Myoclonic / diagnosis
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Epilepsies, Myoclonic / genetics
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Female
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Follow-Up Studies
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Frameshift Mutation
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Humans
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Infant
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Intellectual Disability / etiology
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Language Disorders / etiology
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Mitochondrial Diseases / complications*
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Mitochondrial Diseases / diagnosis
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NAV1.1 Voltage-Gated Sodium Channel / genetics*
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Status Epilepticus / etiology
Substances
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NAV1.1 Voltage-Gated Sodium Channel
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SCN1A protein, human